Lopes Coeli M B, Zhang Hailin, Rohacs Tibor, Jin Taihao, Yang Jian, Logothetis Diomedes E
Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York University, New York, NY 10029, USA.
Neuron. 2002 Jun 13;34(6):933-44. doi: 10.1016/s0896-6273(02)00725-0.
Inwardly rectifying K(+) (Kir) channels are important regulators of resting membrane potential and cell excitability. The activity of Kir channels is critically dependent on the integrity of channel interactions with phosphatidylinositol 4,5-bisphosphate (PIP(2)). Here we identify and characterize channel-PIP(2) interactions that are conserved among Kir family members. We find basic residues that interact with PIP(2), two of which have been associated with Andersen's and Bartter's syndromes. We show that several naturally occurring mutants decrease channel-PIP(2) interactions, leading to disease.
内向整流钾(Kir)通道是静息膜电位和细胞兴奋性的重要调节因子。Kir通道的活性关键取决于通道与磷脂酰肌醇4,5 - 二磷酸(PIP₂)相互作用的完整性。在此,我们鉴定并表征了在Kir家族成员中保守的通道 - PIP₂相互作用。我们发现了与PIP₂相互作用的碱性残基,其中两个与安德森综合征和巴特综合征有关。我们表明,几种天然存在的突变体减少了通道 - PIP₂相互作用,从而导致疾病。